Canonical Allele Identifier: CA1423676461

Gene: PIK3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179234301T= , CM000665.2:g.179234301T=	GRCh38
NC_000003.11:g.178952089T= , CM000665.1:g.178952089T=	GRCh37
NC_000003.10:g.180434783T=	NCBI36
NG_012113.2:g.90779T= , LRG_310:g.90779T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263967.4:c.3144T= MANE Select	ENSP00000263967.3:p.His1048=
ENST00000462255.2:n.2167T=
ENST00000643187.1:c.*224T=	ENSP00000493507.1:n.*224T=
ENST00000674534.1:n.4052T=
ENST00000674622.1:c.1565T=	ENSP00000502417.1:n.1565T=
ENST00000675467.1:n.5951T=
ENST00000675786.1:c.*1711T=	ENSP00000502323.1:n.*1711T=
ENST00000675796.1:n.3039T=
ENST00000263967.3:c.3144T=	ENSP00000263967.3:p.His1048=
NM_006218.2:c.3144T= , LRG_310t1:c.3144T=	NP_006209.2:p.His1048=
XM_006713658.2:c.3144T=	XP_006713721.1:p.His1048=
XM_011512894.1:c.3144T=	XP_011511196.1:p.His1048=
NM_006218.3:c.3144T=	NP_006209.2:p.His1048=
XM_006713658.4:c.3144T=	XP_006713721.1:p.His1048=
XM_011512894.2:c.3144T=	XP_011511196.1:p.His1048=
NM_006218.4:c.3144T= MANE Select	NP_006209.2:p.His1048=